US20100092352A1 - Method and apparatus for producing synthesis gas from waste materials - Google Patents
Method and apparatus for producing synthesis gas from waste materials Download PDFInfo
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- US20100092352A1 US20100092352A1 US12/638,484 US63848409A US2010092352A1 US 20100092352 A1 US20100092352 A1 US 20100092352A1 US 63848409 A US63848409 A US 63848409A US 2010092352 A1 US2010092352 A1 US 2010092352A1
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- reactor
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- devolatilization
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/82—Gas withdrawal means
- C10J3/84—Gas withdrawal means with means for removing dust or tar from the gas
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/48—Apparatus; Plants
- C10J3/485—Entrained flow gasifiers
- C10J3/487—Swirling or cyclonic gasifiers
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/48—Apparatus; Plants
- C10J3/50—Fuel charging devices
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2200/00—Details of gasification apparatus
- C10J2200/15—Details of feeding means
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2200/00—Details of gasification apparatus
- C10J2200/15—Details of feeding means
- C10J2200/154—Pushing devices, e.g. pistons
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2200/00—Details of gasification apparatus
- C10J2200/15—Details of feeding means
- C10J2200/158—Screws
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0903—Feed preparation
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0913—Carbonaceous raw material
- C10J2300/093—Coal
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J2300/00—Details of gasification processes
- C10J2300/09—Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
- C10J2300/0953—Gasifying agents
- C10J2300/0973—Water
Definitions
- Carbonaceous material can be reacted with steam at elevated temperatures to form syn gas, which is a combination of carbon monoxide and hydrogen.
- syn gas which is a combination of carbon monoxide and hydrogen.
- the initial reaction reaches a temperature greater than about 450° F. before the available oxygen is reacted, combustion occurs. This produces unwanted carbon dioxide, ash and slag.
- the temperature must be maintained at 450° F. until after the available oxygen is reacted.
- the present invention is premised on the realization that syn gas can be produced more efficiently by modifying the process disclosed in U.S. Pat. No. 6,863,878, the disclosure of which is hereby incorporated by reference.
- the carbonaceous material in the devolatilization zone is maintained at a temperature less than 450° F. until all of the available oxygen is reacted.
- this material is then raised to a temperature of about 1000° F. in the devolatilization zone prior to being combined with steam to form the syn gas in the reformer reactor.
- the formed syn gas passes through a series of particulate separators to remove any formed ash.
- These separators are maintained at a temperature greater than 1500° F., by housing them in the same furnace as the reformer reactor. This prevents unwanted reactions which can occur when the syn gas cools, and avoids carbon buildup in the apparatus.
- the syn gas from the separator is rapidly quenched to a temperature well below 1000° F., preferably to a temperature of about 120° F. At this temperature, the syn gas is stable and will not form carbon deposits or allow unwanted reactions.
- the material is cooled, preferably in a quencher, any residual tar or oil is separated and either fed back to the devolatilization zone for reaction or collected for further use.
- the heat from the devolatilization zone is directed to a preheater section where water and combustion air are circulated to recover residual heat.
- FIGS. 1A and 1B are diagrammatic depictions of the apparatus used in the present invention.
- FIG. 2 is a cross sectional view of an embodiment of the feed section
- FIG. 3 is a schematic elevational view of an alternate feed section
- FIG. 4 is a plan view of an auger used in the embodiment shown in FIG. 3 .
- syn gas facility 10 includes a feed section 12 which communicates with a devolatilization section 14 , in turn connected to a reformer reactor 16 .
- the reactor 16 is designed to produce syn gas which passes through particulate separators 18 and 20 . The gas is cooled, filtered, and collected for use.
- the feed section 12 includes a hopper 38 having an auger 40 , which directs cabonaceous feed material to feed chamber 42 .
- the feed chamber 42 is connected to a feed tube 44 which leads to the devolatilization section 14 .
- Above the feed section is a cylindrical support 48 which supports a compacting cylinder 46 designed to force feed material from the feed chamber 42 into the feed tube 44 .
- the feed tube 44 leads to a delumper 50 , which communicates via passage 52 to the devolatilization section 14 .
- a gate valve 53 prevents backflow through line 55 from delumper 50 .
- the devolatilization section 14 includes four cylindrical reaction chambers 56 , 58 , 60 and 62 . Each reaction chamber is in communication with the next reaction chamber. Each reaction chamber includes an auger 64 which is adapted to force the feed material through the respective chambers 56 - 62 to feed auger 70 . The augers 64 , in turn, are operated by motors 68 . The feed auger 70 communicates with the feed eductor 72 . Steam from a steam heater 76 located in furnace 77 is introduced into an eductor 72 through steam inlet 74 . This forces material cycloconically through line 75 to the reactor 16 , also located in furnace 77 .
- the furnace 77 includes a burner 78 and a combustion outlet or plenum 80 .
- the furnace includes steam heater 76 and separators 18 and 20 .
- Combustion outlet 80 directs heated air to devolatilization zone 14 , which, in turn, communicates with a preheater 81 which ultimately communicates with a stack 82 .
- reformer reactor 16 is a tubular reactor which communicates with eductor 72 via line 83 .
- An outlet line 84 from reactor 16 leads to the first particulate separator 18 .
- Separator 18 includes a gas outlet line 85 which, in turn, leads to the second particulate separator 20 .
- Line 91 directs gas from separator 20 to a quench eductor 86 which directs gas and water through line 87 to a quench tank 88 ( FIG. 1B ).
- the quench eductor 86 includes a water inlet line 89 .
- the quench tank 88 is a gas/water/oil separator and includes a gas outlet 94 , a water outlet 96 and a tar/oil outlet 98 .
- the tar outlet 98 leads to a pump 100 which directs tar and/or oil via line 102 to line 55 just upstream of delumper 50 .
- the water outlet 96 is directed through line 106 through a surge tank 108 .
- the gas outlet 94 in turn leads to a second quencher eductor 114 , which includes a water inlet 116 directed from tank 117 .
- the quench eductor outlet 118 in turn leads to a secondary quencher 120 .
- the quencher 120 includes a water outlet 122 and a gas outlet 124 , which leads to a quench scrubber 126 .
- the water outlet 122 leads to water line 106 , in turn leading to surge tank 108 .
- the quench scrubber 126 includes a water outlet 128 which goes to a drain 130 .
- the gas outlet 132 from the quench scrubber 126 leads to a T 134 wherein a first line 136 is directed to a water filter 137 which removes water.
- a gas outlet 140 from filter 137 passes to the product gas section 142 , and a water outlet 138 leads via line 128 to drain 130 .
- the second line 146 from T 134 is directed to a second water filter 148 which also includes a water outlet 150 which leads back to the drain 130 via line 128 .
- the gas outlet 152 is directed to a compressor 154 and, in turn, to a scrubber 156 to remove residual water.
- the scrubber 156 includes a water outlet 158 directed to either the drain or makeup water line 244 , and a gas outlet 160 which is, in turn, directed to the burner 78 where it is used to heat the furnace 77 .
- a make up water inlet 200 leads to the surge tank 108 .
- the water in tank 108 can circulate through an optional water treatment package 204 , depending on the particular water conditions, such as hardness and the like.
- the tank 108 includes an outlet 206 which is directed to tandem filters 208 a and 208 b .
- the filters have a common outlet 210 which is directed to T 212 .
- One line from T 212 is directed to a first pump 214 .
- Pump 214 directs the water through line 213 , a filter 216 and, subsequently, to a cooler 218 which directs chilled water back to tank 108 .
- the second line 220 from T 212 is directed to a second T 226 which directs a portion of water to a second pump 228 which directs it to a tank 117 , which, in turn, communicates with a chiller 234 .
- Third pump 230 directs water from T 212 through line 89 into quench eductor 86 , as previously described.
- the apparatus 10 also includes a preheater section 81 which utilizes exhaust gas that has passed from the furnace 77 through the devolatilization section 14 to preheat water for the steam reactor 16 , as well as combustion air for the burner 78 .
- the exhaust from furnace 77 passes through exhaust plenum 80 to devolatilization section 14 and then through exhaust 240 to the preheater section 81 .
- Water inlet line 244 directs deionized water through the preheater section through line 246 to the steam heater 76 .
- a blower 250 is used to introduce air through the preheater 81 . This is exhausted via line 254 to burner 78 .
- feed such as pulverized coal
- feed section 12 is introduced through hopper 38 and feed section 12 where it is compressed by cylinder 46 and forced through valve 53 and line 55 to the delumper 50 .
- the feed is forced into the devolatilization section 14 .
- Cylinder 46 applies sufficient pressure to compress the feed material and drive out most air associated with the feed material, generally 10-20 psi or greater. This force, overcomes any pressure from the devolatilization section and causes the feed material to act as a seal between the feed section 12 and devolatilization section 14 . This removes air from the feed and prevents introduction of unwanted oxygen into the devolatilization zone.
- Auger 64 forces the feed through chambers 56 - 62 .
- the devolatilization section starts with a lower temperature first chamber 56 , followed by a higher temperature second chamber 58 and, in turn, a higher temperature third 60 and fourth 64 chamber.
- the temperatures of the chambers are designed so that the temperature of the feed material does not reach 450° F. until all oxygen in the feed material reacts, in order to prevent pyrolysis.
- the first reaction chamber will have an initial temperature of about 100° F., with the final devolatilization section at 1000° F. Most of the free oxygen will react well before the feed reaches a portion of the devolatilization section that is at 450° F.
- the temperature of each section is controlled by its proximity to exhaust plenum 80 as well as surface area and residence time.
- the pressure from the feed tube 44 through the devolatilization section 14 is about 125 psig.
- the end product exiting from the devolatilization section 14 is primarily char and gases liberated during devolatilization.
- This end product is directed to the feed auger 70 leading to steam eductor 72 .
- Steam from steam heater 76 is directed into the eductor 72 .
- the temperature of the steam should be about 1500° F. and the pressure is about 125 psi.
- the eductor then leads to the reformer reactor 16 wherein the syn gas is created.
- the reactor temperature is increased to greater than 1500° F., preferably about 1550° F. at a pressure of about 125 psig.
- a portion of the reactant flow in reactor 16 can be directed through line 253 to an inlet immediately upstream of feed auger 70 to carry solids at low flow or feed rates.
- the reaction product from reactor 16 ash and syn gas, is directed to cyclone separators 18 and 20 , which are located within the furnace 77 and maintained at the same temperature of the reactor 16 of about 1550° F. at 125 psi. Separators 18 and 20 remove the ash from the reaction product.
- the ash is directed to augers 241 and 243 which move the ash into dry ash bins 245 and 247 without permitting syn gas to escape the system.
- the syn gas flows via line 91 from the furnace to quench eductor 86 and quench tank 88 and where it is cooled to about 120° F. by water from tank 108 at about 140 psi.
- the temperature of the water in tank 108 is controlled by recirculation through cooling tower 218 and is preferably about 90° F.
- the quench tank 88 separates the gas, water, and oil. The water is directed back to tank 108 and is reused.
- the gas itself is then directed from the quench tank 88 to a second quench eductor 114 .
- Water at 200 psi from tank 117 is used to further cool the syn gas to about 70° F. at 125 psi.
- Chiller 234 is used to establish the water temperature at about 60° F.
- the cooled gas flows to the secondary quencher 120 which separates water, directing it back to tank 108 , and allows the gas to flow to quench scrubber 126 , again separating water that is sent through line 128 to the drain from the gas that is directed through filters 137 and 148 .
- the gas from filter 137 is collected for use.
- the gas from filter 148 is fed back to the burner 78 which fuels the furnace.
- a separate fuel source can be used.
- Feeder 250 includes a material hopper 252 having a feed auger 254 leading to feed bin 256 .
- Feed bin 256 includes a screw 258 rotated by motor 260 . The screw leads to feed tube 44 which connects through outlet 262 to the devolatilization section 14 .
- the screw 258 has a main shaft 266 and a helical blade 268 .
- the outer diameter of blade 268 remains constant while the diameter of shaft 266 increases from the inlet portion 220 to the outlet portion 272 . This decreases the area between the shaft 266 and inlet tube 44 , thereby compressing the feed material as it is forced into apparatus 10 . In use, 20-50% preferably 40% compression is preferred.
- the present invention has many different improvements that improve the efficiency of the process disclosed in Klepper U.S. Pat. No. 6,863,878.
- Compressing the feed drives off unwanted air and forms an inlet seal.
- heating the material in a devolatilization zone to 1000° F. prior to addition of steam improves the efficiency of the overall reaction and increases the reaction rate.
- the rapid quenching of the syn gas reaction product further avoids any unwanted carbon deposition or reaction products.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Carbon And Carbon Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Industrial Gases (AREA)
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Abstract
An apparatus designed to form syn gas from carbonaceous materials such as coal includes a devolatilization reactor in combination with a reformer reactor which subsequently forms syn gas. The reformer reactor, in turn, is in communication with a particulate separator. The devolatilization reactor is fed with material using a compression feeder which drives air from the feed material, compresses it in a feed zone forming a seal between the feed hopper and the devolatilization reactor. The reformer reactor, as well as the particulate separators, are maintained in a heated furnace so that the temperature of the formed syn gas does not decrease below the reaction temperature until particulate material has been separated.
Description
- Carbonaceous material can be reacted with steam at elevated temperatures to form syn gas, which is a combination of carbon monoxide and hydrogen. As disclosed in U.S. Pat. No. 6,863,878, if the initial reaction reaches a temperature greater than about 450° F. before the available oxygen is reacted, combustion occurs. This produces unwanted carbon dioxide, ash and slag. To avoid this, as disclosed in U.S. Pat. No. 6,863,878, the temperature must be maintained at 450° F. until after the available oxygen is reacted.
- The present invention is premised on the realization that syn gas can be produced more efficiently by modifying the process disclosed in U.S. Pat. No. 6,863,878, the disclosure of which is hereby incorporated by reference. In particular, the carbonaceous material in the devolatilization zone is maintained at a temperature less than 450° F. until all of the available oxygen is reacted. In the present invention, this material is then raised to a temperature of about 1000° F. in the devolatilization zone prior to being combined with steam to form the syn gas in the reformer reactor.
- From the reformer reactor, the formed syn gas passes through a series of particulate separators to remove any formed ash. These separators are maintained at a temperature greater than 1500° F., by housing them in the same furnace as the reformer reactor. This prevents unwanted reactions which can occur when the syn gas cools, and avoids carbon buildup in the apparatus. The syn gas from the separator is rapidly quenched to a temperature well below 1000° F., preferably to a temperature of about 120° F. At this temperature, the syn gas is stable and will not form carbon deposits or allow unwanted reactions. At the same time the material is cooled, preferably in a quencher, any residual tar or oil is separated and either fed back to the devolatilization zone for reaction or collected for further use. In a further feature of the present invention, the heat from the devolatilization zone is directed to a preheater section where water and combustion air are circulated to recover residual heat.
- The objects and advantages of the present invention will be further appreciated in light of the following detailed description and drawings, in which:
-
FIGS. 1A and 1B are diagrammatic depictions of the apparatus used in the present invention; -
FIG. 2 is a cross sectional view of an embodiment of the feed section; -
FIG. 3 is a schematic elevational view of an alternate feed section; and -
FIG. 4 is a plan view of an auger used in the embodiment shown inFIG. 3 . - As shown diagrammatically in
FIGS. 1A and 16 ,syn gas facility 10 includes afeed section 12 which communicates with adevolatilization section 14, in turn connected to areformer reactor 16. Thereactor 16 is designed to produce syn gas which passes throughparticulate separators - As shown more particularly in
FIGS. 1 and 2 , thefeed section 12 includes ahopper 38 having anauger 40, which directs cabonaceous feed material to feedchamber 42. Thefeed chamber 42 is connected to afeed tube 44 which leads to thedevolatilization section 14. Above the feed section is acylindrical support 48 which supports a compactingcylinder 46 designed to force feed material from thefeed chamber 42 into thefeed tube 44. Thefeed tube 44 leads to adelumper 50, which communicates viapassage 52 to thedevolatilization section 14. Agate valve 53 prevents backflow throughline 55 fromdelumper 50. - The
devolatilization section 14 includes fourcylindrical reaction chambers auger 64 which is adapted to force the feed material through the respective chambers 56-62 to feedauger 70. Theaugers 64, in turn, are operated by motors 68. Thefeed auger 70 communicates with thefeed eductor 72. Steam from asteam heater 76 located infurnace 77 is introduced into aneductor 72 throughsteam inlet 74. This forces material cycloconically throughline 75 to thereactor 16, also located infurnace 77. - The
furnace 77 includes aburner 78 and a combustion outlet orplenum 80. In addition to thereactor 16, the furnace includessteam heater 76 andseparators Combustion outlet 80 directs heated air todevolatilization zone 14, which, in turn, communicates with apreheater 81 which ultimately communicates with astack 82. - As shown,
reformer reactor 16 is a tubular reactor which communicates witheductor 72 vialine 83. Anoutlet line 84 fromreactor 16 leads to thefirst particulate separator 18.Separator 18 includes agas outlet line 85 which, in turn, leads to thesecond particulate separator 20.Line 91 directs gas fromseparator 20 to aquench eductor 86 which directs gas and water through line 87 to a quench tank 88 (FIG. 1B ). Thequench eductor 86 includes awater inlet line 89. - The
quench tank 88 is a gas/water/oil separator and includes agas outlet 94, awater outlet 96 and a tar/oil outlet 98. Thetar outlet 98, as shown, leads to apump 100 which directs tar and/or oil vialine 102 to line 55 just upstream ofdelumper 50. Thewater outlet 96 is directed throughline 106 through asurge tank 108. - The
gas outlet 94 in turn leads to asecond quencher eductor 114, which includes awater inlet 116 directed fromtank 117. Thequench eductor outlet 118 in turn leads to asecondary quencher 120. Thequencher 120 includes awater outlet 122 and agas outlet 124, which leads to aquench scrubber 126. - The
water outlet 122 leads towater line 106, in turn leading tosurge tank 108. Thequench scrubber 126 includes awater outlet 128 which goes to adrain 130. Thegas outlet 132 from thequench scrubber 126 leads to aT 134 wherein afirst line 136 is directed to awater filter 137 which removes water. Agas outlet 140 fromfilter 137 passes to theproduct gas section 142, and awater outlet 138 leads vialine 128 to drain 130. Thesecond line 146 fromT 134 is directed to asecond water filter 148 which also includes awater outlet 150 which leads back to thedrain 130 vialine 128. Thegas outlet 152 is directed to acompressor 154 and, in turn, to ascrubber 156 to remove residual water. Thescrubber 156 includes awater outlet 158 directed to either the drain ormakeup water line 244, and agas outlet 160 which is, in turn, directed to theburner 78 where it is used to heat thefurnace 77. - A make up
water inlet 200 leads to thesurge tank 108. The water intank 108 can circulate through an optionalwater treatment package 204, depending on the particular water conditions, such as hardness and the like. - The
tank 108 includes anoutlet 206 which is directed totandem filters 208 a and 208 b. The filters have acommon outlet 210 which is directed toT 212. One line fromT 212 is directed to afirst pump 214.Pump 214 directs the water throughline 213, afilter 216 and, subsequently, to a cooler 218 which directs chilled water back totank 108. Thesecond line 220 fromT 212 is directed to asecond T 226 which directs a portion of water to asecond pump 228 which directs it to atank 117, which, in turn, communicates with achiller 234.Third pump 230 directs water fromT 212 throughline 89 into quencheductor 86, as previously described. - The
apparatus 10 also includes apreheater section 81 which utilizes exhaust gas that has passed from thefurnace 77 through thedevolatilization section 14 to preheat water for thesteam reactor 16, as well as combustion air for theburner 78. The exhaust fromfurnace 77 passes throughexhaust plenum 80 todevolatilization section 14 and then through exhaust 240 to thepreheater section 81.Water inlet line 244 directs deionized water through the preheater section throughline 246 to thesteam heater 76. Ablower 250 is used to introduce air through thepreheater 81. This is exhausted vialine 254 toburner 78. - In operation, feed, such as pulverized coal, is introduced through
hopper 38 andfeed section 12 where it is compressed bycylinder 46 and forced throughvalve 53 andline 55 to thedelumper 50. The feed is forced into thedevolatilization section 14.Cylinder 46 applies sufficient pressure to compress the feed material and drive out most air associated with the feed material, generally 10-20 psi or greater. This force, overcomes any pressure from the devolatilization section and causes the feed material to act as a seal between thefeed section 12 anddevolatilization section 14. This removes air from the feed and prevents introduction of unwanted oxygen into the devolatilization zone. -
Auger 64 forces the feed through chambers 56-62. The devolatilization section starts with a lower temperaturefirst chamber 56, followed by a higher temperaturesecond chamber 58 and, in turn, a higher temperature third 60 and fourth 64 chamber. The temperatures of the chambers are designed so that the temperature of the feed material does not reach 450° F. until all oxygen in the feed material reacts, in order to prevent pyrolysis. Generally, the first reaction chamber will have an initial temperature of about 100° F., with the final devolatilization section at 1000° F. Most of the free oxygen will react well before the feed reaches a portion of the devolatilization section that is at 450° F. The temperature of each section is controlled by its proximity toexhaust plenum 80 as well as surface area and residence time. The pressure from thefeed tube 44 through thedevolatilization section 14 is about 125 psig. - The end product exiting from the
devolatilization section 14 is primarily char and gases liberated during devolatilization. This end product is directed to thefeed auger 70 leading tosteam eductor 72. Steam fromsteam heater 76 is directed into theeductor 72. The temperature of the steam should be about 1500° F. and the pressure is about 125 psi. The eductor then leads to thereformer reactor 16 wherein the syn gas is created. In thereactor 16, the reactor temperature is increased to greater than 1500° F., preferably about 1550° F. at a pressure of about 125 psig. A portion of the reactant flow inreactor 16 can be directed throughline 253 to an inlet immediately upstream offeed auger 70 to carry solids at low flow or feed rates. - The reaction product from
reactor 16, ash and syn gas, is directed tocyclone separators furnace 77 and maintained at the same temperature of thereactor 16 of about 1550° F. at 125 psi.Separators augers dry ash bins - After passing through
separators line 91 from the furnace to quencheductor 86 and quenchtank 88 and where it is cooled to about 120° F. by water fromtank 108 at about 140 psi. The temperature of the water intank 108 is controlled by recirculation throughcooling tower 218 and is preferably about 90° F. The quenchtank 88 separates the gas, water, and oil. The water is directed back totank 108 and is reused. - The gas itself is then directed from the quench
tank 88 to a second quencheductor 114. Water at 200 psi fromtank 117 is used to further cool the syn gas to about 70° F. at 125 psi.Chiller 234 is used to establish the water temperature at about 60° F. The cooled gas flows to thesecondary quencher 120 which separates water, directing it back totank 108, and allows the gas to flow to quenchscrubber 126, again separating water that is sent throughline 128 to the drain from the gas that is directed throughfilters filter 137 is collected for use. The gas fromfilter 148 is fed back to theburner 78 which fuels the furnace. For initial start up, a separate fuel source can be used. - An
alternate feeder 250 is shown inFIGS. 3 and 4 .Feeder 250 includes amaterial hopper 252 having afeed auger 254 leading to feedbin 256.Feed bin 256 includes ascrew 258 rotated bymotor 260. The screw leads to feedtube 44 which connects throughoutlet 262 to thedevolatilization section 14. - As shown in
FIG. 4 , thescrew 258 has amain shaft 266 and ahelical blade 268. The outer diameter ofblade 268 remains constant while the diameter ofshaft 266 increases from theinlet portion 220 to theoutlet portion 272. This decreases the area between theshaft 266 andinlet tube 44, thereby compressing the feed material as it is forced intoapparatus 10. In use, 20-50% preferably 40% compression is preferred. - Thus, the present invention has many different improvements that improve the efficiency of the process disclosed in Klepper U.S. Pat. No. 6,863,878. Compressing the feed drives off unwanted air and forms an inlet seal. Further, heating the material in a devolatilization zone to 1000° F. prior to addition of steam improves the efficiency of the overall reaction and increases the reaction rate. By maintaining the separators in the furnace and maintaining their temperature, unwanted reactions are avoided, and, in particular, carbon deposition on the apparatus is minimized. The rapid quenching of the syn gas reaction product further avoids any unwanted carbon deposition or reaction products.
- This has been a description of the present invention along with the preferred method of practicing the present invention. However, the invention itself should only be defined by the appended claims, WHEREIN I CLAIM:
Claims (5)
1.-16. (canceled)
17. An apparatus for forming syn gas comprising a devolatilization reactor in communication with a reformer reactor, in turn in communication with a first particulate separator wherein said reformer reactor and said separator are maintained in a furnace.
18. The apparatus claimed in claim 17 further comprising a second particulate separator in communication with said first particulate separator wherein said second particulate separator is also located in said furnace.
19. The apparatus claimed in claim 18 comprising a quencher in communication with said second separator.
20. The apparatus claimed in claim 17 further comprising a compacting feeder which forms a seal between a feed zone and said devolitalization reactor.
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US12/638,484 US20100092352A1 (en) | 2006-03-06 | 2009-12-15 | Method and apparatus for producing synthesis gas from waste materials |
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US11/368,820 US7655215B2 (en) | 2006-03-06 | 2006-03-06 | Method and apparatus for producing synthesis gas from waste materials |
US12/638,484 US20100092352A1 (en) | 2006-03-06 | 2009-12-15 | Method and apparatus for producing synthesis gas from waste materials |
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US11/368,820 Division US7655215B2 (en) | 2006-03-06 | 2006-03-06 | Method and apparatus for producing synthesis gas from waste materials |
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US11/368,820 Expired - Fee Related US7655215B2 (en) | 2006-03-06 | 2006-03-06 | Method and apparatus for producing synthesis gas from waste materials |
US12/638,484 Abandoned US20100092352A1 (en) | 2006-03-06 | 2009-12-15 | Method and apparatus for producing synthesis gas from waste materials |
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US (2) | US7655215B2 (en) |
EP (1) | EP1991640A2 (en) |
JP (1) | JP2009529095A (en) |
CN (1) | CN101395254A (en) |
AR (1) | AR059768A1 (en) |
AU (1) | AU2007223367B2 (en) |
BR (1) | BRPI0708375A2 (en) |
CA (1) | CA2644243A1 (en) |
MX (1) | MX2008011353A (en) |
NZ (2) | NZ570827A (en) |
PE (1) | PE20071279A1 (en) |
SA (1) | SA07280092B1 (en) |
TW (1) | TW200745322A (en) |
WO (1) | WO2007103771A2 (en) |
ZA (1) | ZA200807427B (en) |
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US9227895B2 (en) * | 2007-07-09 | 2016-01-05 | Albemarle Corporation | Methods and apparatus for producing alcohols from syngas |
US8153027B2 (en) * | 2007-07-09 | 2012-04-10 | Range Fuels, Inc. | Methods for producing syngas |
US8142530B2 (en) * | 2007-07-09 | 2012-03-27 | Range Fuels, Inc. | Methods and apparatus for producing syngas and alcohols |
US20090018371A1 (en) * | 2007-07-09 | 2009-01-15 | Range Fuels, Inc. | Methods and apparatus for producing alcohols from syngas |
US20090014689A1 (en) * | 2007-07-09 | 2009-01-15 | Range Fuels, Inc. | Methods and apparatus for producing syngas and alcohols |
US20090151253A1 (en) * | 2007-12-17 | 2009-06-18 | Range Fuels, Inc. | Methods and apparatus for producing syngas and alcohols |
US20100273899A1 (en) * | 2009-04-22 | 2010-10-28 | Range Fuels, Inc. | Integrated, high-efficiency processes for biomass conversion to synthesis gas |
US20100319255A1 (en) * | 2009-06-18 | 2010-12-23 | Douglas Struble | Process and system for production of synthesis gas |
CA2771578A1 (en) | 2009-09-16 | 2011-03-24 | Greatpoint Energy, Inc. | Processes for hydromethanation of a carbonaceous feedstock |
CA2773845C (en) | 2009-10-19 | 2014-06-03 | Greatpoint Energy, Inc. | Integrated enhanced oil recovery process |
AU2010310846B2 (en) | 2009-10-19 | 2013-05-30 | Greatpoint Energy, Inc. | Integrated enhanced oil recovery process |
US8733459B2 (en) | 2009-12-17 | 2014-05-27 | Greatpoint Energy, Inc. | Integrated enhanced oil recovery process |
US20110146978A1 (en) | 2009-12-17 | 2011-06-23 | Greatpoint Energy, Inc. | Integrated enhanced oil recovery process |
JP5615199B2 (en) * | 2011-02-21 | 2014-10-29 | 三菱重工業株式会社 | Combustion device |
EP2983906A4 (en) | 2013-04-08 | 2016-12-28 | Thermochem Recovery Int Inc | Hydraulic feeder system having compression stage with multi-cylinder hydraulic circuit |
CN105987634B (en) * | 2015-01-31 | 2018-09-14 | 中国石油化工股份有限公司 | The supplementing device of water |
US20160223087A1 (en) * | 2015-02-03 | 2016-08-04 | Sustainable Waste Power Systems, Inc. | Control valve system for controlling fluid flow |
US20220002152A1 (en) * | 2020-07-01 | 2022-01-06 | James E. Klepper | System and method for making syngas |
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- 2007-03-02 AU AU2007223367A patent/AU2007223367B2/en not_active Ceased
- 2007-03-02 CN CNA200780007895XA patent/CN101395254A/en active Pending
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Also Published As
Publication number | Publication date |
---|---|
US7655215B2 (en) | 2010-02-02 |
TW200745322A (en) | 2007-12-16 |
BRPI0708375A2 (en) | 2011-06-07 |
NZ587489A (en) | 2011-06-30 |
MX2008011353A (en) | 2008-12-03 |
PE20071279A1 (en) | 2007-12-14 |
CN101395254A (en) | 2009-03-25 |
AU2007223367A1 (en) | 2007-09-13 |
AR059768A1 (en) | 2008-04-30 |
CA2644243A1 (en) | 2007-09-13 |
NZ570827A (en) | 2011-05-27 |
ZA200807427B (en) | 2009-07-29 |
JP2009529095A (en) | 2009-08-13 |
US20070205092A1 (en) | 2007-09-06 |
WO2007103771A2 (en) | 2007-09-13 |
AU2007223367B2 (en) | 2011-04-14 |
EP1991640A2 (en) | 2008-11-19 |
WO2007103771A3 (en) | 2008-01-31 |
SA07280092B1 (en) | 2010-10-12 |
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